A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881505



Internal ID22656481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:90083825..90088529hg38UCSC Ensembl
chr16:90150233..90154937hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg384705
hg194705
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474805, nssv17479799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881505
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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